---
title: "BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net con... — FDA record Z-0008-2025 | Is It on Recall"
description: "The bulk product used in the recalling firm's repackaged finished product was recalled due to bacterial contamination."
url: https://isitonrecall.com/recall/fda-device-z-0008-2025-biotrol-purit-clean-it-general-purpose-ultrasonic-cleaner-ref-pc016-net-contents-16-fl-oz-makes-16-g/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of so... — FDA record Z-0008-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 23, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of solution.
- **Reason**: The bulk product used in the recalling firm's repackaged finished product was recalled due to bacterial contamination.
- **Classification**: Class II
- **Recalling firm**: Young Dental Manufacturing I, LLC
- **Quantity**: 1,391 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0008-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0008-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot numbers 247026, 255361, 234038, and 241667, exp. 6/13/2026; UDI-DI 00302730002089. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Distribution was made to AZ, ID, MD, NV, NY, PA, SC, TN, TX, WI. There was no government/military/foreign distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Idaho](https://isitonrecall.com/state/idaho/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Oct 9, 2024
- **Recall initiation date**: Aug 23, 2024
- **Center classification date**: Oct 1, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0008-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Young Dental Manufacturing I, LLC records](https://isitonrecall.com/brand/young-dental-manufacturing-i-llc/)